Moisture and Ultraviolet Light Barrier Composition

ABSTRACT

A composition for the creation of a protective barrier on a wide variety of materials to prevent the deterioration and degradation caused by exposure to moisture and sun over time.

CROSS REFERENCE TO RELATED APPLICATION(S)

This application is a Continuation of U.S. Utility patent applicationSer. No. 13/839,549, filed Mar. 15, 2013, which in turn claims thebenefit of U.S. Provisional Patent Application Ser. No. 61/649,014,filed May 18, 2012 and U.S. Provisional Patent Application Ser. No.61/613,731, filed Mar. 21, 2012. The entire disclosures of all the aboveapplications are herein incorporated by reference.

BACKGROUND OF THE INVENTION

1. Field of the Invention

This disclosure is related to the field of compositions for the creationof a protective barrier against moisture and ultraviolet light.

2. Description of Related Art

Water and sun are two forces capable of wreaking havoc on a vast numberof material surfaces, causing them to degrade and deteriorate with thepassage of time. For example, water intrusion can enable the attack of amaterial or system by destructive processes such as the rotting of wood,rusting of metals and the de-lamination of plywood, amongst many otherdegrading processes. In addition, sun damage can result in fading andbreakdown in the integrity of materials such as plastics, vinyl andrubber.

The impact of this damage over time on the economy as a whole cannot beunderestimated. For example, the impact of just one of these destructiveprocesses, rust, is immense. Rust is the general colloquial term for aseries of oxides that form on iron and its alloys (such as steel) as aresult of the reaction of iron and oxygen in the presence of water ormoisture. Basically, when iron is in contact with water and oxygen, itrusts. Iron metal is relatively unaffected by pure water or by dryoxygen alone; the combination needs to be present for rust to form. Thisis because a tightly adhering oxide coating, known as a passivationlayer, protects the bulk of the iron from oxidation. It is thepassivating layer itself that converts to rust from exposure to thecombined action of oxygen and water.

Chemically, the rusting of iron is an electrochemical process thatbegins with the transfer of electrons from iron to oxygen:O₂+4e⁻+H₂O→4OH⁻. From this equation, it is illustrated that theoccurrence of corrosion is dictated by the availability of water andoxygen. Further, the rate of corrosion reactions can be accelerated byelectrolytes (this is illustrated by the accelerating effects of roadsalt on rust formation in automobiles).

Because rust is basically a reaction on the passivation layer of theiron substance, the rust layer does not generally adhere or staypermanently attached to the bulk metal substance. Rather, it forms,flakes off the surface and, as it flakes, exposes fresh iron. Generally,given sufficient time, this cyclic corrosion process will continue untilan iron mass will eventually convert entirely to rust and disintegrate.

It is commonly known that the corrosion of metallic structures has asignificant impact on the United States economy, includinginfrastructure, transportation, utilities, production, manufacturing andgovernmental sectors. One of the pioneering benchmark studies on thecost of corrosion performed in 1975 calculated the costs to be about $70billion per year, or about 4.2 percent of the nation's gross domesticproduct (GDP). A more recent study commissioned by the Federal HighwayAdministration (FHWA) in 2001 showed that the cost of corrosion to theoverall American economy had not significantly waned in the interveningdecades. The study determined the direct costs of corrosion to theUnited States economy to be $279 billion per year or about 3.2 percentof the United States GDP. When indirect costs (otherwise known associety costs) to the user were taken into account, the overallcorrosion costs rose to about 6 percent of the GDP. Economic sectorsthat are commonly affected by corrosion and rust formation include, butare not limited to, infrastructure (e.g., highway bridges, gas andliquid transmission pipelines, waterways and ports, hazardous materialsstorage, airports and railroads), utilities (e.g., gas distribution,drinking water and sewer systems, electrical utilities andtelecommunications), transportation (e.g., motor vehicles, ships,aircrafts, railroad cars, and hazardous materials transport), productionand manufacturing (e.g., oil and gas exploration and production, mining,petroleum refining, chemical, petrochemical and pharmaceutical, pulp andpaper, agricultural, food processing, electronics and home appliances)and government (e.g., defense and nuclear waste storage).

Thus, the economic impact of rust on infrastructure systems and theeconomy as a whole is large. Traditionally utilized rust preventiontechniques generally include, but are not limited to, protectivecoatings, corrosion-resistant alloys, corrosion inhibitors, polymers,anodes, cathodic protection and corrosion control and monitoringequipment. However, despite the availability of these corrosion controlmethodologies, the negative impact of corrosion and rust on the UnitedStates economy keeps rising. Obviously, the presently employedstrategies are not enough to win the ever-waging battle against rust.New, more effective methods to combat rust and its growing negativeimpact on the United States economy are therefore needed.

Similar to rust, more viable protection methodologies and solutions arealso needed for other degradation and deterioration processes on a widevariety of materials (e.g., metals, wood, vinyl, plastic) that occurfrom exposure to moisture or sun over time. A new and effectiveprotective composition that would act as a barrier to water and sun forthese materials, protecting them for significant a significant period oftime from these degrading and deteriorating processes, is thereforeneeded.

SUMMARY OF THE INVENTION

Because of these and other problems in the art, described herein, amongother things, is a composition for the creation of a protective barrieron a wide variety of materials to prevent the deterioration anddegradation caused by exposure to moisture and sun over time.

A rust inhibition prevention composition consisting essentially of amixture of: a plant wax; and an animal oil. In one embodiment of therust inhibition prevention composition, the plant wax comprises acarnauba wax and the animal oil comprises a mink oil. In yet anotherembodiment, this rust inhibition composition will further comprise atallow. In still another embodiment, this rust inhibition preventioncomposition will further comprise an emulsifier. In one embodiment thisemulsifier will be chosen from the group consisting of: glycerol estersof fatty acids, glycerol monooleate, Stoddard solvents,1,2,4-trimethylbenzene, mineral spirits, and naptha. In still anotherembodiment, the prevention composition will further comprise a dye. Inanother embodiment, the prevention composition will further comprising amineral oil. In another embodiment, the prevention composition willfurther comprising a fragrance.

Also disclosed herein is a prevention composition comprised of a mixtureof: about 10-20% of a carnauba wax; about 1-8% of a 1,2,4trimethylbenzene; about 10-20% of a glycerol ester of C14, C18 fattyacids; about 1-5% of a mink oil; about 10-20% of a glycerol monooleate;about 1-8% of a tallow; about 25-45% of a Stoddard solvent; about 4-12%of a mineral spirits; and about 0.2-1.5% of a dye.

Another prevention composition is comprised of a mixture of: about10-20% of a carnauba wax; about 1-8% of a 1,2,4 trimethylbenzene; about15-30% of a glycerol ester of C14, C18 fatty acids; about 1-5% of a minkoil; about 15-25% of a glycerol monooleate; about 1-8% of a tallow;about 35-45% of a Stoddard solvent; about 4-12% of a mineral spirits;about 2-7% of a mineral oil; about 2-5% of a fragrance (such as citrus);and about 0.2-1.5% of a dye.

Yet another prevention composition is comprised of a mixture of: about10-20% of a carnauba wax; about 1-8% of a 1,2,4 trimethylbenzene; about15-30% of a glycerol ester of C14, C18 fatty acids; about 1-5% of a minkoil; about 10-20% of a glycerol monooleate; about 1-8% of a tallow;about 35-45% of a Stoddard solvent; about 2-7% of a mineral spirits;about 4-12% of a mineral oil; and about 1-2% of a fragrance (such ascitrus).

Also disclosed herein is a prevention composition comprised of a mixtureof: about 10-20% of a carnauba wax; about 1-8% of a 1,2,4trimethylbenzene; about 15-30% of a glycerol ester of C14, C18 fattyacids; about 1-5% of a mink oil; about 20-30% of a glycerol monooleate;about 1-8% of a tallow; about 35-45% of a Stoddard solvent; about 4-12%of a mineral spirits; and about 0.2-1.5% of a Carbon Black 70 dye.

Still another prevention composition disclosed herein consists of: about10.85% of a carnauba wax; about 2.40% of a 1,2,4 trimethylbenzene; about13.68% of a glycerol ester C14, C18 fatty acids; about 1.85% of a minkoil; about 13.5% of a glycerol monooleate; about 2.8% of a tallow; about28.8% of a Stoddard solvent; about 6.5% of a mineral spirits; about15.7% of a mineral oil; and about 3.92% of a fragrance.

In yet another embodiment, the prevention composition will consist of:about 10.85% of a carnauba wax; about 2.40% of a 1,2,4 trimethylbenzene;about 13.68% of a glycerol ester of C14, C18 fatty acids; about 1.85% ofa mink oil; about 13.5% of a glycerol monooleate; about 2.8% of atallow; about 28.8% of a Stoddard solvent; about 6.5% of a mineralspirits; about 15.7% of a mineral oil; and about 3.92% of a citrusfragrance.

Also disclosed herein is a method for applying a rust inhibitioncomposition to a surface of an object to be treated, the methodcomprising: heating the surface of the object to be treated to atemperature warm enough to melt or liquefy the rust inhibitioncomposition on contact; applying the rust inhibition composition to thesurface of the object to be treated, keeping the surface warm during theapplying; and cooling the surface of the object to be treated back toroom temperature after the step of applying. In one embodiment of thismethod, in the step of heating, the surface of the object to be treatedwill be heated to about 100° F.-140° F. In another embodiment of thismethod, in the step of heating, the surface of the object to be treatedwill be heated to about 120° F.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 provides a chart of the raw materials of an embodiment of themoisture and ultraviolet light barrier composition.

FIG. 2 provides a chart of the raw materials of an alternativeembodiment of the moisture and ultraviolet light barrier composition.

DESCRIPTION OF THE PREFERRED EMBODIMENT(S)

This disclosure is intended to teach by way of example and not by way oflimitation. The present disclosure focuses on a formulation for acomposition which functions as a protective barrier against moisture,ultraviolet rays, stains, deposits, rust and fingerprints and otherknown deteriorating or degrading processes or substances known to thoseof ordinary skill in the art for a wide variety of materials. In oneembodiment, this composition, in a simplified form, is comprised of acombination of waxes and water repellants. Also discussed herein aremethods for the production of such compositions, along with variousalternative methods of using such compounds in the prevention of waterand sun deterioration or other known degrading processes on a widevariety of materials and products.

As noted previously, in its most general format, the compositiondisclosed herein is comprised of a combination of waxes and waterrepellants formed into a mixture. Any type of organic compound with along alkyl chain that is malleable near ambient temperatures and iscommonly known to those of skill in the art as a “wax” is contemplatedas a wax component of the disclosed composition. Contemplated waxesinclude, but are not limited to: plant and animal waxes such as shellacwax, castor wax, carnauba wax and soy wax, petroleum waxes such asparaffin wax, mineral waxes such as ceresin wax, and synthetic waxessuch as polyethylene wax. In certain embodiments, the contemplated waxin the composition is a shoe polish wax blend. Generally, any waxycolloidal emulsion shoe polish comprised of some or all of naptha,lanolin, turpentine, wax, gum Arabic, ethylene glycol and a colorant iscontemplated. In preferred embodiments, the contemplated wax shoe polishwill be comprised of carnauba wax. Commercial examples of contemplatedshoe polish blends include, but are not limited to, Club Classic® pastepolish, a carnauba wax blend. Further, organic water repellents are alsocontemplated as components in the disclosed composition. Generally, anyorganic water repellant known to those of ordinary skill in the art iscontemplated as an organic water repellant component of the disclosedcomposition. Contemplated organic water repellents include animal oils,such as mink oil, and common alternatives thereto known to those ofordinary skill in the art (e.g., macadamia nut oil and sea buckthornoil). However, it should be noted that, in certain embodiments,commercial water repellents could also be utilized.

While the invention is not intended to be limited to any effect of themodality of the deterioration and degradation prevention composition, itis hypothesized that one explanation for the effectiveness of thiscomposition in preventing the deterioration and degradation caused overtime by water and sun in addition to its ability to protect surfacesfrom stains and oily deposits is that the water repellant qualities ofthe wax and water repellent blend impede the water or moisture necessaryfor deterioration and degradation to occur from coming into contact withthe surface area of a treated material. Further, the barrier formed byapplication of the composition on the material can also act as a barrierto ultraviolet rays, preventing these rays from coming into directcontact with the material, which direct contact results in a breakdownof the material over time.

In one embodiment of the disclosed prevention composition, thecomposition comprises: carnauba wax and mink oil. In another embodimentof the disclosed prevention composition, the composition consists of:carnauba wax and mink oil. In yet another embodiment of the disclosedcomposition, the composition consists essentially of: a plant wax andanimal oil. In still another embodiment of the disclosed composition,the composition consists essentially of: a palm wax and an animal oil.In another embodiment of the disclosed composition, the compositionconsists essentially of: a carnauba wax and mink oil. In yet anotherembodiment of the disclosed composition, the composition consistsessentially of: carnauba wax blend and mink oil. In more complexembodiments of the disclosed composition, the composition is furthercomprised of tallow such as, but not limited to, bleached tallow. Thisfurther component adds, amongst other properties, lubrication propertiesto the resultant composition.

In another embodiment, the composition is further comprised of certainemulsifiers and solvents known to those of ordinary skill in the art.Contemplated emulsifiers and solvents include, but are not limited to,glycerol esters of fatty acids, glycerol monooleate, Stoddard solvents,1,2,4-trimethylbenzene, mineral spirits, and naptha. However, it shouldbe noted that this list is not exclusive, as any emulsifier or solventknown to those of ordinary skill in the art is contemplated as apossible component of the disclosed composition. Further, in anotherembodiment, the disclosed composition is further comprised of a dyeknown to those of ordinary skill in the art that is compatible withsilicon and wax type materials such as, but not limited to, carbonblack. Notably, the color of the dye is not determinative; the color ofthe dye can vary depending upon how and upon what material thecomposition will be utilized. In one embodiment where the dye is black,the resultant composition will be black. In yet another embodiment, thecomposition will be further comprised of a mineral oil known to those ofordinary skill in the art and a contemplated fragrance. Contemplatedfragrances include, but are not limited to, fruit, plant, flower andfreshener scents known to those of ordinary skill in the art.

Generally, contemplated ranges for certain components of the compositionin various different embodiments are as follows: about 10-20% carnaubawax blend; about 1-8% 1,2,4 trimethylbenzene; about 10-20% glycerolester of C14, C18 fatty acids; about 1-5% of mink oil; about 10-20%glycerol monooleate; about 1-8% tallow; about 25-45% Stoddard solvent;about 4-12% mineral spirits/naptha; and about 0.2-1.5% carbon black dye.In a preferred embodiment of the composition, the specific percentagesof the components are as follows: about 15% carnauba wax; about 3% 1,2,4trimethylbenzene; about 15% glycerol ester of C14, C18 fatty acids;about 2% of mink oil; about 14.6% glycerol monooleate; about 3% tallow;about 40% Stoddard solvent; about 7% mineral spirits/naptha; and about0.4% carbon black dye. FIG. 1 provides a chart of the raw materials ofan embodiment of this specific preferred embodiment of the disclosedprevention composition. Notably, however, in no way is this listing ofranges and specific percentages intended to be exhaustive, as otherranges could be contemplated in additional embodiments of thecomposition.

In an alternative embodiment of the prevention and inhibitioncomposition, generally for use in the home-goods industry amongst otherapplications, the specific percentages of the components are as follows:about 10.85% carnauba wax blend; about 2.40% 1,2,4 trimethylbenzene;about 13.68% glycerol ester of C14, C18 fatty acids; about 1.85% minkoil; about 13.5% glycerol monooleate; about 2.8% tallow; about 28.8%Stoddard solvent; about 6.5% mineral spirits/naptha; about 15.7% mineraloil; and about 3.92% citrus fragrance.

Generally, the prevention and inhibition composition disclosed hereinmay take any form known to those of ordinary skill in the art now or inthe future for protective barriers and prevention coatings or inhibitorsincluding, but not limited to: a cream, a paste, a solution, a liquid, alotion, an ointment and/or a gel.

In certain embodiments, the prevention and inhibition composition willbe applied as follows. First, the surface of the object to be treatedwill be heated to a temperature warm enough to melt or liquefy the rustprevention and inhibition composition on contact. In one embodiment,this will be about 100° F.-140° F., preferably about 120° F. Then, theprevention and inhibition composition will be added to the surface ofthe object to be treated, keeping the surface warm during theapplication. In one embodiment, this application will occur with asoft-bristle brush. Once the application is complete, the treated objectwill be allowed to cool back to normal room temperature. In other modesof application, the surface of the object to be treated will not beheated; the composition will simply be applied by another methodologyknown to those of ordinary skill in the art that does not require apreheating of the material surface (e.g., spreading, brushing, spraying,etc. to a room temperature surface).

In other embodiments, in particular for the embodiment of the preventionand inhibition composition for the home-goods industry, the compositionis applied to the desired surface with a soft cloth, paper towel,sponge, brush or other application mechanism known to those of ordinaryskill in the art. After application, the desired surface will be wipedor buffed clean. This application process can be repeated as needed.Desired surfaces for application include, but are not limited to,stainless steel, glass, leather, vinyl, cardboard, copper, sterlingsilver, fiberglass, aluminum and brass.

In one embodiment, the disclosed prevention composition is created bythe following process. In a first step, the carnauba wax blend, 1,2,4trimethylbenzene, glycerol ester of C14-C18 fatty acid, mink oil,glycerol monooleate, bleached tallow, Stoddard solvent, mineralspirits/naptha and carbon black dye are all heated by a method known tothose of ordinary skill in the art until they liquefy. In one embodimentof this first step, the carnauba wax will be liquefied by placing aquantity of the carnauba wax (such as 5 gallons) into a heatingmechanism (such as a heat box) which is heated to a temperature of about175° F. for about 5-6 hours. In another embodiment of this first step,the 1,2,4 trimethylbenzene, glycerol ester of C14-C18 fatty acid, minkoil, glycerol monooleate, bleached tallow, Stoddard solvent, mineralspirits/naptha and carbon black dye will all be placed into a heatingmechanism known to those of ordinary skill in the art (such as an oven)which is heated to about 140° F.-145° F.

In a second step, a container is heated to about 140° F.-200° F., in apreferred embodiment to about 175° F. Generally, any container orheating mechanism known to those of ordinary skill in the art iscontemplated. In one embodiment, an aluminum or stainless steelcontainer is utilized. In another embodiment, the container is heated tothe applicable temperature by placing the container over heated coils.In a third step, the carnauba wax is added to the pre-heated container.In this step, the carnauba wax is maintained at a temperature within therange of about 140° F.-200° F., preferably about 175° F. for a period ofabout 30 minutes. In one embodiment of this step, the carnauba wax willbe stirred by a stirring mechanism known to those of ordinary skill inthe art at regular time intervals, in one embodiment at three (3) minutetime intervals.

In a fourth step, the glycerol monooleate, Stoddard solvent, mineralspirits and naptha will be added to the carnauba wax and the temperatureof the mixture will be maintained at within the range of about 140°F.-200° F., preferably about 175° F. for a period of about 3-5 minutes.In one embodiment of this step, the mixture will be stirred by astirring mechanism known to those of ordinary skill in the art for acertain time period, in one embodiment for about 30 seconds. In a fifthstep, the carbon black dye is added to the mixture. In one embodiment ofthis step, the mixture will be stirred by a stirring mechanism known tothose of ordinary skill in the art for a certain time period, in oneembodiment for about 1-2 minutes.

In a sixth step, the mixture will be maintained at a temperature withinthe range of about 140° F.-200° F., preferably about 175° F. for acertain time period. In a preferred embodiment, the mixture will bemaintained at a temperature within the range of about 140° F.-200° F.,preferably about 175° F. for about five (5) minutes. At the end of thisallocated time period, in a seventh step, the mixture will be stirred bya stirring mechanism known to those of ordinary skill in the art.

In an eighth step, the resultant mixture will be dispensed and allowedto cool and cure to room temperature by methods known to those ofordinary skill in the art. In one embodiment of the disclosed process,about 640 ounces of the carnauba wax; about 31.60 ounces of animal oil;about 31.60 ounces of trimethylbenzene, Stoddard solvent and naptha(equal parts combined and about 2.25 ounces of carbon black 70 dye) willbe utilized.

In the alternative embodiment of the prevention composition for thehome-goods industry, another contemplated method for creating thecomposition is as follows. First, the carnuba wax, trimethylbenzene andStoddard solvent are combined and heated to about 175° F. In a secondstep, the glycerol esters, animal oil, glycerol monooleate and bleachedtallow are heated separately from the first combination to about 140° F.In a third step, the second combination is added to the firstcombination. In a fourth step, the mineral spirits are heated to about140° F. and added to the mix. In a fifth step, the mineral oil is addedand mixed. In a sixth step, the fragrance is added. In a seventh step,the mixture is heated to about 170° F. and stirred for about 5 minutes.In a final step, the resultant mixture is dispensed and allowed to cooland cure to room temperature by methods known to those of ordinary skillin the art.

The advantages of the disclosed prevention composition are its abilityto act as a protective barrier against moisture and ultraviolet rays forthe material upon which it is applied, thereby inhibiting and preventingthe deterioration and degradation caused by these elements over time,even in extreme conditions.

For example, preliminary testing has shown that the disclosedcomposition has the ability to prevent the formation of rust in numerousextreme conditions including thermal shock conditions, 1000 hour saltfog (60% solution) conditions, acid exposure conditions, abrasivetesting conditions, and salt spray (92% solution) conditions. In each ofthe preliminary testing environments, the disclosed composition wasapplied to a steel tie rod end followed by an adequate cure time knownto those of ordinary skill in the art. Following the cure period, thetreated rod was exposed to each of the preliminary testing environmentsas follows:

Thermal Shock Test

In the thermal shock test, a treated rod was exposed to extremetemperatures within the range of about −140° F. to 135° F. for about 10hours. Specifically, in this test the component was heated to 135° F.and then the temperature was cycled to about −140° F. at variousintervals, ranging from about 5 minutes to about 1 hour. This cyclictemperature change was repeated for about 10 hours. The completion ofthe 10 hour thermal shock test revealed no measurable degree ofdeterioration, corrosion or discoloration of the treated rod. In thistest, the composition provided 100% durability.

1000 Hour Salt Fog (60% Solution) Test

In the salt fog test, a treated rod was exposed to about a 60% saltsolution for about 1000 hours. Specifically, in this test the componentwas placed in a salt fog chamber for about 1000 hours and exposed to a60% salt solution. After the completion of the test, the treated rod wasremoved and inspected visually and with a magnifying scope. Theinspection revealed no measurable degree of deterioration, discoloring,corrosion, or degradation to the coating or the treated rod. Thus, theprevention composition provided remarkable protection and corrosionresistance, providing 100% corrosion protection and durability.

Acid Exposure Test

In the acid exposure test, a treated rod was exposed to a hydrochloricacid solution for about ½ hour. Specifically, in this test the treatedrod was placed in a sealed chamber and exposed to a diluted solution of38% hydrochloric acid. As known to those of ordinary skill in the art, adiluted solution of hydrochloric acid will quickly rust mild steelcomponents. The treated rod was then exposed to an intermittent spray ofthe diluted acid solution for about ½ hour. Upon completion of the test,the treated rod was removed for inspection. The inspection revealed nomeasurable degree of deterioration, discoloring or corrosion; theprevention composition had provided 100% protection and durability.Further, the inspection revealed that the acid solution remained on thesurface of the treated rod without any measurable penetration of thecoating of the disclosed prevention composition.

Abrasive (Impact) Test

In the abrasive (impact) test, a treated rod was exposed to simulatedabrasive materials for about an hour. In this test, the treated rod wasplaced in a sealed chamber and exposed to a variety of differentmaterials including but not limited to ground glass, sand and rock forabout an hour. The abrasive materials were generally applied to thetreated rod at about 30 psi from a distance of about 17 mm.After-testing inspection revealed that the treated rod was not damagedduring the testing, no visible signs of damage or pitting were evidentin the coating of the prevention material or on the rod. In sum, thetreated rod showed 100% durability in this test.

Salt Spray Test (92% Solution)

In the salt spray test, a treated rod was exposed to a salt spraysolution which contained about 92% brine solution for about 60 hours atabout 15 psi spray pressure and about 60 percent humidity. Notably, thisis an extremely high solution of salt saturation. Specifically, in thetest the treated rod was placed in a salt spray container containingabout a 92% Brine solution. The treated rod was exposed to the 92%solution for about 60 hours with a 15 psi spray pressure during thetest. An inspection following the test revealed no measurable degree ofdeterioration, discoloring or corrosion. The 92% salt spray (a highlyconcentrated solution with properties that will quickly corrode metal)test revealed that the prevention composition provided excellentprotection from the corrosive effects of the testing solution; 100%protection and durability was demonstrated upon inspection.

In sum, these preliminary test results reveal the remarkable protectionand durability from moisture provided to iron and iron alloys by theprevention composition disclosed herein. This same protection from thedamage caused by moisture and sunlight is also believed provided toother materials upon which the composition is applied including but notlimited to metals (e.g., stainless steel, iron, aluminum, preciousmetals, etc.), plastics, vinyl, wood, rubber and any other materialsthat are at risk for deterioration and degradation from exposure tomoisture and ultraviolet rays over time. Further, the disclosedcomposition can also be utilized for other useful functions to preventcertain moistures, oils or other substances from coming into contactwith treated materials. The prevention of fingerprints and smudges onstainless steel coated with the disclosed composition is one suchexample. The prevention of deterioration from acid rain on treatedmetals and other materials is another example.

While the invention has been disclosed in conjunction with a descriptionof certain embodiments, including those that are currently believed tobe the preferred embodiments, the detailed description is intended to beillustrative and should not be understood to limit the scope of thepresent disclosure. As would be understood by one of ordinary skill inthe art, embodiments other than those described in detail herein areencompassed by the present invention. Modifications and variations ofthe described embodiments may be made without departing from the spiritand scope of the invention.

1. A method for applying a rust inhibition composition to a surface ofan inorganic object to be treated, the method comprising: heating thesurface of the inorganic object to be treated to a temperature warmenough to melt or liquefy the rust inhibition composition on contact;applying the rust inhibition composition to the heated surface of theinorganic object to be treated, keeping the surface warm during theapplying; and cooling the surface of the inorganic object to be treatedback to room temperature after the step of applying; wherein the rustinhibition prevention composition comprises of a mixture of: about10-20% of a carnauba wax; about 1-8% of a 1,2,4 trimethylbenzene; about15-30% of a glycerol ester of C14, C18 fatty acids; about 1-5% of a minkoil; about 15-25% of a glycerol monooleate; about 1-8% of a tallow;about 35-45% of a Stoddard solvent; about 4-12% of a mineral spirits;about 2-7% of a mineral oil; about 2-5% of a fragrance; and about0.2-1.5% of a dye.
 2. The method of claim 1 wherein said fragrance is acitrus fragrance.
 3. A method for applying a rust inhibition compositionto a surface of an inorganic object to be treated, the methodcomprising: heating the surface of the inorganic object to be treated toa temperature warm enough to melt or liquefy the rust inhibitioncomposition on contact; applying the rust inhibition composition to theheated surface of the inorganic object to be treated, keeping thesurface warm during the applying; and cooling the surface of theinorganic object to be treated back to room temperature after the stepof applying; wherein the rust inhibition prevention compositioncomprises of a mixture of: about 10-20% of a carnauba wax; about 1-8% ofa 1,2,4 trimethylbenzene; about 15-30% of a glycerol ester of C14, C18fatty acids; about 1-5% of a mink oil; about 10-20% of a glycerolmonooleate; about 1-8% of a tallow; about 35-45% of a Stoddard solvent;about 2-7% of a mineral spirits; about 4-12% of a mineral oil; about1-2% of a fragrance; and about 0.2-1.5% of a dye.
 4. The method of claim3 wherein said fragrance is a citrus fragrance.
 5. A method for applyinga rust inhibition composition to a surface of an inorganic object to betreated, the method comprising: heating the surface of the inorganicobject to be treated to a temperature warm enough to melt or liquefy therust inhibition composition on contact; applying the rust inhibitioncomposition to the heated surface of the inorganic object to be treated,keeping the surface warm during the applying; and cooling the surface ofthe inorganic object to be treated back to room temperature after thestep of applying; wherein the rust inhibition prevention compositioncomprises of a mixture of: about 10-20% of a carnauba wax; about 1-8% ofa 1,2,4 trimethylbenzene; about 15-30% of a glycerol ester of C14, C18fatty acids; about 1-5% of a mink oil; about 20-30% of a glycerolmonooleate; about 1-8% of a tallow; about 35-45% of a Stoddard solvent;about 4-12% of a mineral spirits; and about 0.2-1.5% of a dye.
 6. Themethod of claim 5 wherein said dye is Carbon Black 70.